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Ex Vivo Equine Cartilage Explant Osteoarthritis Model: A Metabolomics and Proteomics Study
[Image: see text] Osteoarthritis is an age-related degenerative musculoskeletal disease characterized by loss of articular cartilage, synovitis, and subchondral bone sclerosis. Osteoarthritis pathogenesis is yet to be fully elucidated with no osteoarthritis-specific biomarkers in clinical use. Ex vi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7476031/ https://www.ncbi.nlm.nih.gov/pubmed/32701294 http://dx.doi.org/10.1021/acs.jproteome.0c00143 |
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author | Anderson, James R. Phelan, Marie M. Foddy, Laura Clegg, Peter D. Peffers, Mandy J. |
author_facet | Anderson, James R. Phelan, Marie M. Foddy, Laura Clegg, Peter D. Peffers, Mandy J. |
author_sort | Anderson, James R. |
collection | PubMed |
description | [Image: see text] Osteoarthritis is an age-related degenerative musculoskeletal disease characterized by loss of articular cartilage, synovitis, and subchondral bone sclerosis. Osteoarthritis pathogenesis is yet to be fully elucidated with no osteoarthritis-specific biomarkers in clinical use. Ex vivo equine cartilage explants (n = 5) were incubated in tumor necrosis factor-α (TNF-α)/interleukin-1β (IL-1β)-supplemented culture media for 8 days, with the media removed and replaced at 2, 5, and 8 days. Acetonitrile metabolite extractions of 8 day cartilage explants and media samples at all time points underwent one-dimensional (1D) (1)H nuclear magnetic resonance metabolomic analysis, with media samples also undergoing mass spectrometry proteomic analysis. Within the cartilage, glucose and lysine were elevated following TNF-α/IL-1β treatment, while adenosine, alanine, betaine, creatine, myo-inositol, and uridine decreased. Within the culture media, 4, 4, and 6 differentially abundant metabolites and 154, 138, and 72 differentially abundant proteins were identified at 1–2, 3–5, and 6–8 days, respectively, including reduced alanine and increased isoleucine, enolase 1, vimentin, and lamin A/C following treatment. Nine potential novel osteoarthritis neopeptides were elevated in the treated media. Implicated pathways were dominated by those involved in cellular movement. Our innovative study has provided insightful information on early osteoarthritis pathogenesis, enabling potential translation for clinical markers and possible new therapeutic targets. |
format | Online Article Text |
id | pubmed-7476031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-74760312020-09-08 Ex Vivo Equine Cartilage Explant Osteoarthritis Model: A Metabolomics and Proteomics Study Anderson, James R. Phelan, Marie M. Foddy, Laura Clegg, Peter D. Peffers, Mandy J. J Proteome Res [Image: see text] Osteoarthritis is an age-related degenerative musculoskeletal disease characterized by loss of articular cartilage, synovitis, and subchondral bone sclerosis. Osteoarthritis pathogenesis is yet to be fully elucidated with no osteoarthritis-specific biomarkers in clinical use. Ex vivo equine cartilage explants (n = 5) were incubated in tumor necrosis factor-α (TNF-α)/interleukin-1β (IL-1β)-supplemented culture media for 8 days, with the media removed and replaced at 2, 5, and 8 days. Acetonitrile metabolite extractions of 8 day cartilage explants and media samples at all time points underwent one-dimensional (1D) (1)H nuclear magnetic resonance metabolomic analysis, with media samples also undergoing mass spectrometry proteomic analysis. Within the cartilage, glucose and lysine were elevated following TNF-α/IL-1β treatment, while adenosine, alanine, betaine, creatine, myo-inositol, and uridine decreased. Within the culture media, 4, 4, and 6 differentially abundant metabolites and 154, 138, and 72 differentially abundant proteins were identified at 1–2, 3–5, and 6–8 days, respectively, including reduced alanine and increased isoleucine, enolase 1, vimentin, and lamin A/C following treatment. Nine potential novel osteoarthritis neopeptides were elevated in the treated media. Implicated pathways were dominated by those involved in cellular movement. Our innovative study has provided insightful information on early osteoarthritis pathogenesis, enabling potential translation for clinical markers and possible new therapeutic targets. American Chemical Society 2020-07-23 2020-09-04 /pmc/articles/PMC7476031/ /pubmed/32701294 http://dx.doi.org/10.1021/acs.jproteome.0c00143 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Anderson, James R. Phelan, Marie M. Foddy, Laura Clegg, Peter D. Peffers, Mandy J. Ex Vivo Equine Cartilage Explant Osteoarthritis Model: A Metabolomics and Proteomics Study |
title | Ex Vivo Equine Cartilage Explant
Osteoarthritis Model: A Metabolomics and Proteomics Study |
title_full | Ex Vivo Equine Cartilage Explant
Osteoarthritis Model: A Metabolomics and Proteomics Study |
title_fullStr | Ex Vivo Equine Cartilage Explant
Osteoarthritis Model: A Metabolomics and Proteomics Study |
title_full_unstemmed | Ex Vivo Equine Cartilage Explant
Osteoarthritis Model: A Metabolomics and Proteomics Study |
title_short | Ex Vivo Equine Cartilage Explant
Osteoarthritis Model: A Metabolomics and Proteomics Study |
title_sort | ex vivo equine cartilage explant
osteoarthritis model: a metabolomics and proteomics study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7476031/ https://www.ncbi.nlm.nih.gov/pubmed/32701294 http://dx.doi.org/10.1021/acs.jproteome.0c00143 |
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